J. LEVY

ORCID: 0000-0003-1677-5217
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About
Contact & Profiles
Research Areas
  • Chemical synthesis and alkaloids
  • Alkaloids: synthesis and pharmacology
  • Asymmetric Synthesis and Catalysis
  • Oxidative Organic Chemistry Reactions
  • Synthesis and Reactions of Organic Compounds
  • Synthesis and Biological Evaluation
  • Traditional and Medicinal Uses of Annonaceae
  • Fluorine in Organic Chemistry
  • Nonlinear Optical Materials Research
  • Synthesis and pharmacology of benzodiazepine derivatives
  • Chemical Synthesis and Reactions
  • Crystal structures of chemical compounds
  • Plant-based Medicinal Research
  • Synthetic Organic Chemistry Methods
  • Organic Chemistry Cycloaddition Reactions
  • Analytical Chemistry and Chromatography
  • Synthesis of Organic Compounds
  • Chemical Synthesis and Analysis
  • Molecular spectroscopy and chirality
  • Synthesis of Indole Derivatives
  • Cancer Treatment and Pharmacology
  • Carbohydrate Chemistry and Synthesis
  • Phytochemistry and Biological Activities
  • Botanical Research and Chemistry
  • Advanced Condensed Matter Physics

Centre National de la Recherche Scientifique
1990-2024

École nationale des ponts et chaussées
2024

Laboratoire Techniques, Territoires et Sociétés
2024

Laboratoire de Cristallographie et Sciences des Matériaux
1982-2004

Université Joseph Fourier
1990-2002

Université Grenoble Alpes
1990-2002

Université de Reims Champagne-Ardenne
1990-2000

Laboratoire de Cristallographie et RMN Biologiques
1977-1997

Unité Matériaux et Transformations
1974-1987

Centre Hospitalier Universitaire de Reims
1976

Encapsulation of an optically nonlinear octupolar guanidinium cation in a host polyanionic L-monohydrogentartrate lattice leads to noncentrosymmetric orthorhombic P2 1 2 guest-host crystalline structure with cell parameters a=11.347 (2), b=11.162 c=6.668 (2) A Z=4. Final R=0.049 from 1229 independent reflections. The packing shows strong interlocking between the anionic and cationic sublattices by multidirectional hydrogen-bonding network. optimally oriented for 222 crystal point group is...

10.1107/s0108768192008395 article EN Acta Crystallographica Section B Structural Science 1993-04-01

New noncentrosymmetric crystals including the 2-amino-5-nitropyridinium and 2-amino-5-nitropyridine chromophores have been designed following a strategy first applied to dihydrogen phosphate. If counteranion able self-aggregate in chains or layers as (H2PO4-)n is associated cation, structure based on herringbone motifs systematically formed. In same way it has observed that bulky group grafted amine radical of induces containing molecular entities. The structures dichloroacetate ionic...

10.1021/cm9501731 article EN Chemistry of Materials 1996-01-01

2-Amino-5-nitropyridinium halides have been synthesized and their crystal structures determined. The of acentric phases reveal networks non-linear chromophores arranged in herringbone motifs. Their secondharmonic generation responses vary magnitude between that 3-methyl-4-nitropyridine N-oxide 2-methyl-2,4-dinitrophenyl aminopropanoate molecular compounds. Chained anions screen favourably the interactions cations phases, while reverse situation is observed centric phase...

10.1039/jm9930300999 article EN Journal of Materials Chemistry 1993-01-01
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